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<h5 class="section-title" id="d8762495e233">BACKGROUND</h5>
<p id="P2">Criteria for identification of anatomic ventricular tachycardia (VT) substrates
in
arrhythmogenic right ventricular cardiomyopathy (ARVC) on late gadolinium enhancement
(LGE) cardiac magnetic resonance (CMR) are unclear.
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<h5 class="section-title" id="d8762495e238">OBJECTIVE</h5>
<p id="P3">We sought to define a) the association of regional RV epicardial voltage
amplitude
with the distribution of LGE, and b) appropriate image signal intensity (SI) thresholds
for VT substrate identification, in ARVC.
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<h5 class="section-title" id="d8762495e243">METHODS</h5>
<p id="P4">Pre-procedural LGE-CMR and epicardial electrogram mapping were performed
in 10 ARVC
patients. The location of epicardial electrogram map points, obtained during sinus
rhythm with intrinsic conduction or RV pacing, were retrospectively registered to
the corresponding LGE image regions. Standardized SI z-scores (standard deviation
distance from the mean) were calculated for each 10-mm region surrounding map points.
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<h5 class="section-title" id="d8762495e248">RESULTS</h5>
<p id="P5">In patient-clustered, generalized estimating equations models that included
3205 epicardial
EAM points and corresponding SI measures, bipolar (−1.43 mV/z-score,
<i>P</i> < 0.001) and unipolar voltage amplitude (−1.22 mV/z-score,
<i>P</i> < 0.001) were associated with regional SI z-scores. In contrast to the
QRS-LP interval
(
<i>P</i> =0.362), the LP activation index (LPAI) defined as electrogram duration divided
by
QRS-LP was associated with regional SI z-scores (
<i>P</i> < 0.001). SI z-score thresholds of >0.05 [95% confidence interval (CI),
−0.05–0.15]
and < −0.16 (95% CI, −0.26–0.06) corresponded to bipolar voltage measures <0.5
and
>1.0 mV, respectively.
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<h5 class="section-title" id="d8762495e265">CONCLUSION</h5>
<p id="P6">Increased RV gadolinium uptake is associated with lower epicardial bipolar
and unipolar
electrogram voltage amplitude. Standardized LGE-CMR SI z-scores may augment pre-procedural
planning for identification of low voltage zones and abnormal myocardium in ARVC.
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